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Pain, Postoperative clinical trials

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NCT ID: NCT04995497 Completed - Clinical trials for Erector Spinae Plane Block

Intravenous(IV) vs. Erector Spinae Plane Blocks in Cardiac Surgery

Start date: August 15, 2021
Phase: Phase 2
Study type: Interventional

Interfascial plane blocks have been developed for analgesia, among which the erector spinae plane (ESP) has gained popularity. The ESP block has been hypothesized to provide truncal analgesia by spread of local anesthetic into the paravertebral space. Recent studies have contested this idea showing unreliability in the spread of the local anesthetic into the paravertebral space.

NCT ID: NCT04993521 Completed - Postoperative Pain Clinical Trials

Ultrasound Guided Bilateral Superficial Cervical Plexus Block in Patients Undergoing Total Thyroidectomy.

BSCPB_Block
Start date: February 1, 2019
Phase: N/A
Study type: Interventional

The present study compared the efficacy of bilateral superficial cervical plexus block (BSCPB) versus local wound infiltration (LWI) regarding the postoperative opioid consumption in patients undergoing total thyroidectomy

NCT ID: NCT04990700 Completed - Pain, Postoperative Clinical Trials

Effect of Partial Rib Resection On the Control of Post-thoracotomy Pain

Start date: May 9, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effect of partial rib resection in reducing acute post-thoracotomy pain

NCT ID: NCT04988893 Completed - Post Operative Pain Clinical Trials

Quality of Recovery Scores in Parturients With Obesity

Start date: August 9, 2021
Phase:
Study type: Observational

The prevalence of obesity has increased dramatically recently. Obesity is a pro-inflammatory state which leads to chronic low grade inflammation having different systemic effects. This may make obesity an independent risk factor for severe acute postoperative pain. No prospective studies have been conducted to specifically evaluate the quality of recovery after caesarean delivery for women with morbid obesity when compared to non-obese parturients. In addition, while there is biological plausibility to infer worse pain scores in parturients with obesity, the magnitude of this difference is unknown and information guiding adjustments in pain management are lacking.

NCT ID: NCT04988776 Completed - Postoperative Pain Clinical Trials

PECS II Versus ICBN Block Plus SCNB for AV Fistula Creation in CRF Patients

Start date: February 1, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

Brachial plexus block (BPB) is often utilized for proximal arm arteriovenous access creation. However, the medial upper arm and axilla are often inadequately anesthetized, as the Intercostobrachial nerve (which provides sensory supply to the axilla, upper medial arm, and a small area at the upper lateral chest) is not a component of the brachial plexus. This requires repeated, an intraoperative local anesthetic (LA) supplementation up to conversion into GA. The intercostobrachial nerve (ICBN) is a purely sensory nerve that arises primarily from the second intercostal nerve (T2) with occasional contribution from T3. Therefore, It is not a component of the brachial plexus and is not anesthetized by brachial plexus blockade. The ICBN can be blocked together with other nerves, such as the pectoral, intercostal, and long thoracic nerves in a recently described technique named pectoral nerves block type II (PECS II ).In this thesis, investigators compared the use of the PECS II block and ICBN block as a supplement to supraclavicular brachial plexus block for providing complete anesthesia of the upper arm for fistula creation surgery.

NCT ID: NCT04988490 Recruiting - Cancer Clinical Trials

Quantification of Cannabinoids and Comparison to Post-Surgical Pain Medication Requirements and Surgical Outcomes

Start date: September 22, 2021
Phase:
Study type: Observational

To determine how daily cannabis use affects surgical outcomes.

NCT ID: NCT04984122 Completed - Clinical trials for Procedure, Gynecologic Surgical

Anesthesia on Postoperative Pain After Loop Electrosurgical Excision Procedure

Start date: August 9, 2021
Phase: N/A
Study type: Interventional

The loop electrosurgical excision procedure (LEEP) is a modified cervical conization that is performed with an electrosurgical loop. It may be performed under local anesthesia (LA) or under general anesthesia (GA), and practice patterns differ widely. In some countries, specific guidelines for the choice of anesthesia during LEEP are provided, whereas, in other countries, the choice of anesthesia is not specified. LEEP under LA is more economical, obviating the need for anesthesia staff, equipment, and operating room fees. However, LEEP under LA may be more difficult to perform, may be more difficult to learn, may lead to inferior surgical results, and may result in more pain and patient dissatisfaction. This study aimed to compare loop electrosurgical excision procedures under local anesthesia vs general anesthesia regarding patients' satisfaction, histopathologic results, and short-term morbidity

NCT ID: NCT04984109 Completed - Pain, Postoperative Clinical Trials

Ultrasound-guided PENG Block in Total Hip Replacement

Start date: August 2, 2021
Phase: N/A
Study type: Interventional

- This randomized controlled study will be carried out on 60 adult patients undergoing primary total hip replacement in Tanta University Hospitals. All Patients will receive spinal anesthesia with either sham or real US-guided PENG block. - The primary outcome will be the time to first request for rescue analgesia. The secondary outcome will be the postoperative Numeric Rating Scale (NRS) score and the total morphine consumption (rescue analgesia) in the first 24 h postoperatively.

NCT ID: NCT04983524 Completed - Necrotic Pulp Clinical Trials

Propolis Versus Calcium Hydroxide on Post-Operative Pain in Patients With Necrotic Pulp

Start date: October 2015
Phase: N/A
Study type: Interventional

Propolis is a resinous product of honeybees. Propolis is said to be effective against resistant microorganisms inside the root canal compared to the gold standard medication known as calcium hydroxide. The clinical trial tests the effect of propolis versus calcium hydroxide on pain in patients with necrotic teeth.

NCT ID: NCT04981236 Completed - Postoperative Pain Clinical Trials

Pericapsular Nerve Group (PENG) Block Versus Periarticular Injection for Pain Management After Total Hip Arthroplasty

Start date: August 17, 2021
Phase: N/A
Study type: Interventional

Adequate pain control after total hip arthroplasty is crucial for early ambulation and patient satisfaction. The pericapsular nerve group (PENG) block has been recently introduced a new technique for blockade of the articular branches of the femoral, obturator and accessory obturator nerves. PENG block provides sufficient analgesia but it is still the potential for quadriceps weakness that might delay ambulation. Periarticular injection has attached attention as an effective analgesic modality with a low prevalence of adverse effects. The investigators will compare ultrasound-guided PENG block with periarticular injection in patients undergoing total hip arthroplasty.